Medical
Dental
Vision
Life
Retirement
PTO
... RAVE EDC, DS Navigator, SAS Programming, Reporting and Analytics, Siebel CTMS, Documentum ... Medidata CTMS, BioClinica CTMS, ArisGlobal CTMS) 3) eTMF Solutions (i.e. VEEVA, Documentum ...
Medical
Dental
Vision
Life
Retirement
PTO
... RAVE EDC, DS Navigator, SAS Programming, Reporting and Analytics, Siebel CTMS, Documentum ... Medidata CTMS, BioClinica CTMS, ArisGlobal CTMS) 3) eTMF Solutions (i.e. VEEVA, Documentum ...
Bachelor's degree in Life Sciences, Computer Science, Engineering, Information Systems, Data ... Experience with Rave Medidata or similar EDC platforms * Experience integrating IxRS and EDC ...
Quick apply
Bachelor's degree in Life Sciences, Computer Science, Engineering, Information Systems, Data ... Experience with Rave Medidata or similar EDC platforms * Experience integrating IxRS and EDC ...
$11.86 - $16.95
4% of jobs
$16.95 - $22.04
9% of jobs
$25.70 is the 25th percentile. Wages below this are outliers.
$22.04 - $27.13
17% of jobs
$27.13 - $32.22
13% of jobs
The median wage is $35.19 / hr.
$32.22 - $37.31
13% of jobs
$37.31 - $42.40
10% of jobs
$42.40 - $47.49
9% of jobs
$48.44 is the 75th percentile. Wages above this are outliers.
$47.49 - $52.58
9% of jobs
$52.58 - $57.67
7% of jobs
$57.67 - $62.76
6% of jobs
$62.76 - $67.85
4% of jobs
$11
$39
$67
A Medidata Rave Programmer is responsible for designing, developing, and managing electronic data capture (EDC) systems using Medidata Rave, a widely used clinical trial software. They create study databases, build edit checks, program custom functions, and ensure data integrity for clinical trials. Their role is essential in streamlining data collection, validation, and reporting for regulatory compliance and efficient trial management.
As a Medidata Rave Programmer, your daily tasks often involve designing and programming electronic case report forms (eCRFs), managing edit checks, and customizing the study database in the Medidata Rave platform. You'll collaborate closely with clinical data managers, biostatisticians, and other stakeholders to ensure accurate data capture and compliance with study protocols. Routine responsibilities may also include troubleshooting technical issues, validating builds, and supporting user testing. This role offers a balance of independent programming work and teamwork, providing opportunities to contribute directly to successful clinical trials.
To thrive as a Medidata Rave Programmer, you need strong programming skills, experience in electronic data capture (EDC) for clinical trials, and a background in life sciences or a related field. Expertise with Medidata Rave software, familiarity with Rave Architect, and knowledge of relevant clinical data standards or CDISC certification are highly valuable. Attention to detail, effective communication, and problem-solving abilities help you excel in both independent and collaborative environments. These skills and qualities ensure accurate database builds, smooth study execution, and successful teamwork within clinical research settings.
The most popular types of Medidata Rave Programmer jobs in California are:
For Medidata Rave Programmer jobs in California, the most frequently searched job titles are:
The top searched job categories for Medidata Rave Programmer jobs in California are:
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Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 17 days ago
About Collabera:
Established in 1991, Collabera is one of the fastest growing end-to-end information technology services and solutions companies globally. As a half a billion dollar IT company, Collabera's client-centric business model, commitment to service excellence and Global Delivery Model enables its global 2000 and leading mid-market clients to deliver successfully in an increasingly competitive marketplace.
With over 8200 IT professionals globally, Collabera provides value-added onsite, offsite and offshore technology services and solutions to premier corporations. Over the past few years, Collabera has been awarded numerous accolades and Industry recognitions including.
Collabera awarded Best Staffing Company to work for in 2012 by SIA. (hyperlink here)
Collabera listed in GS 100 - recognized for excellence and maturity
Collabera named among the Top 500 Diversity Owned Businesses
Collabera listed in GS 100 & ranked among top 10 service providers
Collabera was ranked:
32 in the Top 100 Large Businesses in the U.S
18 in Top 500 Diversity Owned Businesses in the U.S
3 in the Top 100 Diversity Owned Businesses in New Jersey
3 in the Top 100 Privately-held Businesses in New Jersey
66th on FinTech 100
35th among top private companies in New Jersey
http://www.collabera.com/about_us/accolades.jsp
Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Collabera offers a full range of benefits to its employees including paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance, Disability Insurance.
Job Description for Clinical Solutions Project Manager - Contract position
Oversight and management of Clinical Trial systems used by Clinical Research organization
Program and Project Management for Clinical Systems projects including system updates, enhancements, and new system implementation
Author project documentation including Project Charters, Business Requirements etc...
Develop and present Clinical System strategies and roadmaps.
Partner with global Clinical Research functions to identify business needs and propose new/enhance existing clinical system solutions.
Drive adoption of and facilitate change management of clinical systems in the global Clinical Research function
Develop and Conduct clinical systems training for Global Business End Users
Manage System Vendor relationships.
Provide global production support activities
Skills - Program Management, Project Management, Technology Strategy, SDLC, Business Process Modeling, Vendor Management, User Adoption, System Training, Business Analysis
Clinical Research Functional Experience - Data Management, Clinical Safety, Biostatistics
Systems Experience - RAVE EDC, DS Navigator, SAS Programming, Reporting and Analytics, Siebel CTMS, Documentum
equirements
BA or BS degree in technical or scientific discipline required.
8+ years of experience implementing systems in GxP controlled environment including responsibility for the implementation of either an EDC, Safety or CTMS system.
Strong interpersonal and communication skills; ability to interact with different levels of management.
Experience with implementation of CTMS tool highly desired.
Clinical Research experience in the Medical Device/Pharma industry is a plus.
Skills
1) Project Management
2) Business Analysis
3) Business Process Modeling
4) Clinical Technology Strategy
5) User Adoption
6) System Training
7) Vendor Management
Systems Experience
1) RAVE EDC
2) CTMS (preferably Oracle CTMS, Medidata CTMS, BioClinica CTMS, ArisGlobal CTMS)
3) eTMF Solutions (i.e. VEEVA, Documentum, NextDocs)
4) Safety Database
5) Reporting and Analytics
6) DS Navigator
7) SAS Programming
All your information will be kept confidential according to EEO guidelines.
